ArticleThe Journal of veterinary medical science2026
Re-maturation of canine chemically-induced hepatic progenitor cells toward biliary epithelial cells.
Article in The Journal of veterinary medical science, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
10 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
This study aimed to evaluate the differentiation potential of canine hepatic progenitor cells (cHPCs) derived from cryopreserved hepatocytes (cHeps). The cHeps were reprogrammed using three small molecules, Y-27632, A-83-01, and CHIR99021, to establish cHPCs. The cells were cultured on Matrigel in a chemically defined feeder-free maintenance medium for human pluripotent stem cells containing YAC, followed by 2% growth factor-reduced Matrigel. During culture, cHPCs transitioned from two-dimensional sheets to three-dimensional ductal structures. qRT-PCR and immunohistochemistry revealed increased CK19 expression on the ductal surfaces, indicating biliary epithelial-like differentiation. Overall, cHPCs possess a bipotential rematuration capacity. This study demonstrated that cHPCs induced by the YAC cocktail possess bipotent differentiation capabilities, confirming that their characteristics are likely to chemically induce liver progenitor cells.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.